46195
Farnesylacetone
technical, mixture of stereo isomers, ≥90% (GC)
Synonym(s):
6,10,14-Trimethyl-5,9,13-pentadecatrien-2-one
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About This Item
Empirical Formula (Hill Notation):
C18H30O
CAS Number:
Molecular Weight:
262.43
EC Number:
212-097-9
UNSPSC Code:
12352100
PubChem Substance ID:
Beilstein/REAXYS Number:
1781239
MDL number:
Assay:
≥90% (GC)
InChI key
LTUMRKDLVGQMJU-UHFFFAOYSA-N
InChI
1S/C18H30O/c1-15(2)9-6-10-16(3)11-7-12-17(4)13-8-14-18(5)19/h9,11,13H,6-8,10,12,14H2,1-5H3
SMILES string
C\C(C)=C\CCC(C)=CCCC(C)=CCCC(C)=O
grade
technical
assay
≥90% (GC)
refractive index
n20/D 1.481
density
0.88 g/mL at 20 °C (lit.)
Storage Class
10 - Combustible liquids
wgk
WGK 2
flash_point_f
230.0 °F - closed cup
flash_point_c
110 °C - closed cup
ppe
Eyeshields, Gloves
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Substrate specificity of undecaprenyl pyrophophate synthetase from Lactobacillus plantarum.
Baba T and Allen Jr CA.
Biochemistry, 17(26), 5598-5604 (1978)
Geonseek Ryu et al.
Archives of pharmacal research, 26(10), 796-799 (2003-11-12)
Two known farnesylacetone derivatives (1 and 2) were isolated from the Korean brown alga Sargassum sagamianum off Jeju Island, Korea. Compounds 1 and 2 were identified as (5E,10Z)-6,10,14-trimethylpentadeca-5,10-dien-2,12-dione and (5E,9E,13E)-6,10,4-trimethyl-pentadeca-5,9,13-trien-2,12-dione, respectively, by comparison with the literature data. Compounds 1 and
Inhibition of transmethylases by unsaturated carbonyl derivatives.
M Rojas et al.
Die Naturwissenschaften, 67(12), 607-608 (1980-12-01)
Catalytic Epoxypolyene Cyclization via Radicals: A Simple Total Synthesis of Sclareol Oxide and its 8Epimer.
Gansauer A, et al.
Synthesis, 2151-2154 (2006)
Byong-Gon Park et al.
Bioorganic & medicinal chemistry letters, 18(24), 6324-6326 (2008-11-14)
Two farnesylacetones, 311 and 312, major active constituents of Sargassum siliquastrum collected from the coast of the East Sea in Korea, showed a moderate vasodilatation effect on the basilar arteries of rabbits. Therefore, treatment with farnesylacetones 311 and 312 may
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